JPS6413069A - Optically active mono-beta-lactam ring derivative and production thereof - Google Patents

Optically active mono-beta-lactam ring derivative and production thereof

Info

Publication number
JPS6413069A
JPS6413069A JP62166624A JP16662487A JPS6413069A JP S6413069 A JPS6413069 A JP S6413069A JP 62166624 A JP62166624 A JP 62166624A JP 16662487 A JP16662487 A JP 16662487A JP S6413069 A JPS6413069 A JP S6413069A
Authority
JP
Japan
Prior art keywords
formula
beta
production
optically active
compound expressed
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP62166624A
Other languages
Japanese (ja)
Inventor
Masahiro Kajiwara
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shiseido Co Ltd
Original Assignee
Shiseido Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shiseido Co Ltd filed Critical Shiseido Co Ltd
Priority to JP62166624A priority Critical patent/JPS6413069A/en
Publication of JPS6413069A publication Critical patent/JPS6413069A/en
Pending legal-status Critical Current

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  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

NEW MATERIAL:A compound expressed by formula I (either of R1 and R2 is H and the other is -CH2COCH3). USE:An intermediate for antibiotic substances. PREPARATION:A compound expressed by formula II (either of R1 and R2 is H and the other is OH) is reacted with a compound expressed by formula III (Y is Cl, Br or I) or formula IV and the resultant compound is then subjected to ring opening using a ring opening reaction reagent, such as a compound expressed by formula V. The obtained compound is subsequently reacted with triphenylphosphine and diethyl carbonate in THF to afford the aimed compound expressed by formula I.
JP62166624A 1987-07-03 1987-07-03 Optically active mono-beta-lactam ring derivative and production thereof Pending JPS6413069A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62166624A JPS6413069A (en) 1987-07-03 1987-07-03 Optically active mono-beta-lactam ring derivative and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62166624A JPS6413069A (en) 1987-07-03 1987-07-03 Optically active mono-beta-lactam ring derivative and production thereof

Publications (1)

Publication Number Publication Date
JPS6413069A true JPS6413069A (en) 1989-01-17

Family

ID=15834740

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62166624A Pending JPS6413069A (en) 1987-07-03 1987-07-03 Optically active mono-beta-lactam ring derivative and production thereof

Country Status (1)

Country Link
JP (1) JPS6413069A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6124122A (en) * 1998-07-24 2000-09-26 Samsung Fine Chemicals Co., Ltd. Process for preparing optically pure (S)-3-hydroxy-γ-butyrolactone
EP1084099A1 (en) * 1998-06-01 2001-03-21 Michigan State University Process for the preparation of protected 3-amino-1,2-dihydroxypropane acetal and derivatives thereof
US6713290B2 (en) 1998-07-24 2004-03-30 Samsung Fine Chemicals Co., Ltd. Process for preparing optically pure (S)-3-hydroxy-γ-butyrolactone

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1084099A1 (en) * 1998-06-01 2001-03-21 Michigan State University Process for the preparation of protected 3-amino-1,2-dihydroxypropane acetal and derivatives thereof
EP1084099A4 (en) * 1998-06-01 2001-07-25 Univ Michigan State Process for the preparation of protected 3-amino-1,2-dihydroxypropane acetal and derivatives thereof
US6124122A (en) * 1998-07-24 2000-09-26 Samsung Fine Chemicals Co., Ltd. Process for preparing optically pure (S)-3-hydroxy-γ-butyrolactone
US6221639B1 (en) 1998-07-24 2001-04-24 Samsung Fine Chemicals Co., Ltd. Process for preparing optically pure(S)-3,4-dihydroxybutyric acid derivatives
US6251642B1 (en) 1998-07-24 2001-06-26 Samsung Fine Chemicals, Co., Ltd. Continuous process for preparing optically pure (S)-3-hydroxy-γ-butyrolactone
US6288272B1 (en) 1998-07-24 2001-09-11 Samsung Fine Chemicals Co., Ltd. Continuous process for preparing optically pure (s)-3,4-dihydroxybutyric acid derivatives
US6713290B2 (en) 1998-07-24 2004-03-30 Samsung Fine Chemicals Co., Ltd. Process for preparing optically pure (S)-3-hydroxy-γ-butyrolactone

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